Please use this identifier to cite or link to this item: http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/988
Title: Synthesis of D-Fructose-Based Bifunctional Primary Amine-Thiourea Organocatalysts and Their Applications in Asymmetric Reactions
Authors: Vanlaldinpuia, K
Keywords: carbohydrates; bifunctional thiourea; organocatalyst; enantioselective; Michael addition; aldol reaction
Issue Date: 16-Sep-2023
Citation: Lalhmangaihzuala, S.; Khiangte, V.; Laldinpuii, Z.; Nunnemi, L.; Malsawmsanga, J.; Lallawmzuali, G.; Liana, T.; Lalhriatpuia, C.; Pachuau, Z.; Vanlaldinpuia, K. Synthesis of D-Fructose-Based Bifunctional Primary Amine-Thiourea Organocatalysts and Their Applications in Asymmetric Reactions. Chemistry 2023, 5, 2362–2375. https://doi.org/ 10.3390/chemistry5040156
Abstract: The preparation of a new class of six bifunctional thiourea organocatalysts having a Dfructose scaffold and a primary amino group was demonstrated. In the present study, the novel organocatalysts exhibited excellent enantio- and moderate diastereoselectivities in the asymmetric Michael addition of aliphatic ketones and 1,3-diketone to substituted nitroolefins at room temperature. In addition, the direct asymmetric aldol reaction between cyclic aliphatic ketone and aromatic aldehydes was also studied in the presence of the saccharide-thiourea organocatalysts giving excellent yield with moderate enantioselectivity.
URI: http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/988
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